ライフサイエンスコーパス: YFP

1 YFP expression in roots transformed with pER8 was low ev

2 YFP fluorescence was normal in pOpOff2 transformed roots

3 YFP fusions demonstrate that all 3 proteins are located

4 YFP H-line and Thy1-GCaMP transgenic mice were used in t

5 YFP(+) BMCs in thy1-YFP mice have immunophenotypic featu

6 YFP-tagged, nonglycosylated beta2 displayed mobility kin

7 Using IL-12p40 YFP (Yet40) reporter mice, we show that CD103(+)CD11b(-)

8 cells expressing RyR2(Ser-2367-CFP/Tyr-2801-YFP).

9 ategy based on the bifunctional mCherry-2xCL-YFP-Vpr construct, in which 2xCL denotes a tandem cleava

10 Using a non-mobile version of STM (2xNLS-YFP-STM), we show that STM mobility is required to suppr

11 We analyzed a YFP-COP1-expressing transgenic line and endogenous COP1

12 Full-length NCX1 (FL-NCX1) and a YFP fusion protein of the NCX1 large intracellular loop

13 transport as determined by localization of a YFP-ATG8 reporter and its vacuolar cleavage during nitro

14 s also induced aggregation of alpha-syn*A53T-YFP in cultured cells, whereas none of six Parkinson's d

15 ellow fluorescent protein (alpha-syn140*A53T-YFP) and TgM83(+/-) mice expressing alpha-synuclein (A53

16 on the C-terminal side of Cys-739 abolished YFP-NCX1 palmitoylation.

17 Adolescent YFP-H mice were studied after 6-8 h of sleep (S = 6), sp

18 ying fusion genes for channelrhodopsin-2 and YFP, in either the rostral or caudal regions of the intr

19 ssion of tau or synuclein fusions to CFP and YFP, and confirmed its sensitivity and specificity to ta

20 fied biosensor enhanced FRET between CFP and YFP, consistent with heavy metal-induced folding of MT-I

21 patterns of the 4 subsets defined by GFP and YFP expression, especially concerning chemokine and cyto

22 Expression of the reporter genes (GFP and YFP) was also confirmed using reverse transcription-PCR

23 ns and dynamics of FM4-64-labeled lipids and YFP-tagged transmembrane (TM) proteins in tobacco (Nicot

24 nked with CFP (cyan fluorescent protein) and YFP (yellow fluorescent protein) at N-terminus and C-ter

25 ndocrine cells expressing both serotonin and YFP, whereas single serotonin labeling was observed in 3

26 immunosuppressive action of BMCs (YFP(+) and YFP(-)) was evaluated in an allogenic mixed lymphocyte r

27 with wild-type, Y14D, or Y14F Cav1-CFP and -YFP constructs that FRET efficiency was greater with Y14

28 BRCA2-GFP and -YFP were compared to distinguish diffusion from fluoroph

29 and C-termini-tagged APP constructs: CFP-APP-YFP [containing the fluorescent tags, cyan fluorescent p

30 oducing free mCherry and the core-associated YFP-Vpr.

31 w and cyan fluorescent fusion proteins, AT1R-YFP and BK-CFP, displayed robust co-localized Forster re

32 relative abundance of cells expressing AUX1-YFP in the assayed population.

33 was developed that showed BR-inducible BES1-YFP accumulation in the nucleus, which was decreased in

34 SUPPRESSOR1-yellow fluorescent protein (BES1-YFP) transgenic line was developed that showed BR-induci

35 Expression of the BES1-YFP reporter was strong in the auricle region of develop

36 erfere with incorporation of expressed beta2-YFP subunit into AP-2 or alter AP-2 deposition at surfac

37 rthermore, a drop in FRET efficiency between YFP and mCherry because of cleavage of the bifunctional

38 The immunosuppressive action of BMCs (YFP(+) and YFP(-)) was evaluated in an allogenic mixed l

39 ing prolines impaired palmitoylation of both YFP-NCX1 and FL-NCX1.

40 In dark-grown seedlings, both YFP-COP1 and endogenous COP1 accumulated in the nucleus

41 otein (YFP) is often used as an acceptor but YFP is prone to photobleaching and pH changes.

42 Apoe(-/-) Cx3cr1(GFP) Cd11c(YFP) mice have 4 groups of macrophages in their aortas.

43 ans, we show that IL-10 production by CD4(+) YFP(+) T cells is controlled systemically during malaria

44 ite exhibiting comparable phenotypes, CD4(+) YFP(+) GFP(+) T cells from the liver and lung produced s

45 Mature splenic CD4(+) YFP(+) GFP(+) T cells, which preferentially expressed hi

46 ein (GFP) reporter mice, we show that CD4(+) YFP(+) T cells are the major source of IL-10 in both lym

47 plenic counterparts, showing that the CD4(+) YFP(+) GFP(+) T cells exert graded functions in distinct

48 CD4(+)YFP(+)GFP(+) T cells generally exhibited a short-lived e

49 In contrast, CD4(+)YFP(+)GFP(-) T cell-derived cells expanded rapidly and u

50 that primary malaria infection-induced CD4(+)YFP(+)GFP(+) T cells have limited memory potential, do n

51 Consistently, the surviving CD4(+)YFP(+)GFP(+) T cell-derived cells were unresponsive and

52 ness analysis confirmed actin-dependent CD44-YFP clusters on living cells.

53 al while over-expressing GFP-CENH3 and CENH3-YFP in callus and plants is not and can be partly deposi

54 For GFP-CENH3 and CENH3-YFP, the fused tags at the termini probably affect the s

55 line stably expressing alpha-syn (A53T)-CFP/YFP fusion proteins to detect alpha-syn seeds in brain e

56 We produced dual CFP/YFP-tagged GluA2 subunit constructs that had normal acti

57 a Src-mediated conformational change in CFP/YFP-tagged WT-Cav1 pairs.

58 tein (YFP) and SST-channelrhodopsin 2 (ChR2)-YFP mice, we quantified the impact of SST-NTS neurons on

59 urrents were reliably obtained from SST-ChR2-YFP neurons (n = 16) and the stimulation-response charac

60 Furthermore, using Thy1-ChR2-YFP mice we demonstrate the application of our probes in

61 anced yellow fluorescence protein (VGAT-ChR2-YFP)-expressing mice and a novel fibreoptic 'laserspritz

62 firmed using a second reporter gene, Citrine YFP.

63 transgenic plants harboring CML38pro::CML38:YFP followed by liquid chromatography-tandem mass spectr

64 is end we used targeted expression of a COI1-YFP transgene in the coi1-1 mutant background.

65 We show that expression of COI1-YFP in the epidermis of the stamen filament and anther i

66 blocks of spinal cord, we also assessed CST-YFP mice for 3D imaging and found that YFP fluorescence

67 aging and found that YFP fluorescence in CST-YFP mice is faint for clearing-based 3D imaging in compa

68 he nonspecific and faint YFP labeling in CST-YFP mice limits their utility for assessments of CST axo

69 We show here that in CST-YFP mice, some YFP-labeled axons are not from the CST.

70 al cord, and it was suggested that these CST-YFP mice would be useful for studies of CST regeneration

71 eta-glucuronidase (GUS) activity and DAO1pro:YFP-DAO1 signals, and transformation with DAO1pro:YFP-DA

72 AO1 signals, and transformation with DAO1pro:YFP-DAO1 complemented the mutant phenotypes.

73 r prolonged collagen stimulation, both DDR1b-YFP and DDR2-GFP formed filamentous structures consisten

74 lls expressing full-length DDR2-GFP or DDR1b-YFP.

75 Injection of diphtheria toxin deleted YFP(+) cells from Foxl1-Cre;Rosa(YFP/iDTR) mice and prev

76 ssing the first 126 amino acids, TAN1-DeltaI-YFP, failed to rescue the double mutant phenotype, while

77 sing a conserved middle region, TAN1-DeltaII-YFP, significantly rescued the mutant phenotype in terms

78 meristems and TIBA-pin apices activated DR5:YFP expression with similar kinetics; however, only lfs

79 f the auxin reporters pPIN1:PIN1:GFP and DR5:YFP Upon auxin microapplication, both lfs meristems and

80 revealed a similar distribution of all EphA2-YFP variants in cells.

81 The expression of EphA2-YFP variants and their kinase activity (phosphorylation

82 n labeling was observed in 36% and exclusive YFP labeling in 9%.

83 tif (GZ variant: G540I, G544I) and expressed YFP-tagged EphA2 (WT, HR, and GZ variants) in HEK293T ce

84 None of the tumor nodules expressed YFP, indicating that Foxl1-expressing cells are not the

85 ung carcinoma cell line H1299 that expresses YFP-tagged alpha1 from its normal genomic localization.

86 graphy, to intact mammalian cells expressing YFP-rhTRIM5alpha and found the presence of hexagonal net

87 Overall, the nonspecific and faint YFP labeling in CST-YFP mice limits their utility for as

88 pal gliogenesis (P2-P4), significantly fewer YFP+ cells were evident in the cortex, corpus callosum,

89 purified from brains of transgenic His6-FLAG-YFP-NL2 mice showed enrichment in the Gene Ontology term

90 We find the His6-FLAG-YFP-NL2 to be a suitable tag, with the unamplified YFP s

91 The non-fluorescent YFP variant sREACh is an efficient acceptor, which is us

92 We also find that a functional YFP-QueE fusion localizes to the division septum in fila

93 Native expression of a functional YFP:FEA4 fusion recapitulated this pattern of expression

94 ansfer was observed from an N-terminal-fused YFP to a FRET acceptor, ReAsH (resorufin arsenical hairp

95 In contrast, 25/26KR Gag-YFP bound specifically to the PM, suggesting a role for

96 Unlike 29/31KT Gag-YFP, 29/31KR Gag-YFP was predominantly cytosolic and showed little intrac

97 ent PM-specific localization for 29/31KR Gag-YFP, suggesting that the blocking of PM binding is more

98 ow fluorescent protein (YFP) and 29/31KT Gag-YFP bound nonspecifically to the PM and intracellular me

99 Unlike 29/31KT Gag-YFP, 29/31KR Gag-YFP was predominantly cytosolic and sho

100 using Gag expression constructs (Gag or Gag-YFP, where YFP is yellow fluorescent protein) created fr

101 GFP and GFP+YFP+ macrophages extend and retract dendritic processes,

102 labeled cells in the spinal gray matter have YFP-labeled projections into the spinal cord white matte

103 ges from source cells expressing either hetN-YFP or hetN alone, despite a lack of intercellular excha

104 a lack of intercellular exchange of the HetN-YFP fusion protein.

105 linked to yellow fluorescent protein (hSGLT1-YFP), hSGLT2-YFP and hSGLT3-YFP in oocytes of Xenopus la

106 low fluorescent protein (hSGLT1-YFP), hSGLT2-YFP and hSGLT3-YFP in oocytes of Xenopus laevis, injecte

107 protein (hSGLT1-YFP), hSGLT2-YFP and hSGLT3-YFP in oocytes of Xenopus laevis, injected hRS1-Reg(S20E

108 In bigenic L126Z/WT-hSOD1:YFP mice, disease was not accelerated and WT-hSOD1:YFP r

109 ce, disease was not accelerated and WT-hSOD1:YFP remained diffusely distributed.

110 used to yellow fluorescent protein (WT-hSOD1:YFP) with G37R-hSOD1 produced earlier disease, and spina

111 Mitochondria in CFP-RIG-I:YFP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:Y

112 Using IFNbeta/YFP reporter mice, we identify these IFN-beta-producing

113 ds, we explored the relationship between Il7(YFP+) TECs and mTECs.

114 ures, the thymocyte-induced reduction in Il7(YFP+) TECs dissociates from the receptor activator of NF

115 As the frequency of Il7(YFP+) TECs gradually declines as mTEC development unfold

116 Still, Il7(YFP+) TECs can generate some CD80(+) mTECs in a stepwise

117 letions on the N-terminal side of Cys-739 in YFP-NCX1 did not affect NCX1 palmitoylation, with the ex

118 e and the absence of Vipp1, no difference in YFP expression was observed, which shows that Vipp1 is n

119 broblast activation protein was evidenced in YFP-positive cells in the heart after MI.

120 The expression in YFP-positive cells of fibroblast markers was determined

121 Control mice revealed an increase in YFP(+) neurons and dendrite formation over time.

122 e Mef2 KO mice also displayed an increase in YFP(+) neurons over time-but with significantly stunted

123 fraction of YFP-positive cortical neurons in YFP(J16) mice cortex were identified as callosal project

124 ter mice (messenger of IFN-beta) resulted in YFP(+) and eGFP(+) single-positive cells, whereas among

125 the C terminus of each protein, resulting in YFP complementation and a bright fluorescent signal.

126 ly blocked the increase in REM sleep seen in YFP controls.

127 In YFPs, the pi-stacking of the chromophore with Tyr203 red

128 n of an intact fluorescent protein including YFP when its two complementary, non-fluorescent N- and C

129 bryos, we recovered 616 verified independent YFP-positive lines representing protein traps in 374 gen

130 arized light to bleach and probe an internal YFP-FliN fusion, we show that the innermost components o

131 rrow cells transduced with a MSCV-HOXB4-ires-YFP vector.

132 Coupling of functional data from AtCruA ISD-YFP fusions with statistical analysis of the physiochemi

133 beled within the helical domain (Galphai-L91-YFP) largely do not dissociate upon activation, yet stil

134 However, mitochondria in CFP-LGP2:YFP-LGP2 cells had lower FRET signal in the presence of

135 rotein of the NCX1 large intracellular loop (YFP-NCX1) were expressed in HEK cells.

136 rbored significantly higher numbers of Lrig1/YFP epithelial cells that coexpressed UEA1 (surface cell

137 induced in Lrig1-CreERT2/+;R26R-YFP/+ (Lrig1/YFP) mice that were uninfected or subsequently infected

138 (Myh11-CreERT2) were crossed with Rosa26-LSL-YFP mice for lineage tracing analysis.

139 plants expressing the mutant phyB(Lys996Arg)-YFP photoreceptor are hypersensitive to red light, (ii)

140 essing intrinsic factor (chief cell marker), YFP (lineage marker), and GSII lectin (spasmolytic polyp

141 A maximum YFP/CFP FRET ratio of 2.8 was observed in the presence o

142 cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had higher FRET efficiencies in the prese

143 ndria in CFP-RIG-I:YFP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had higher F

144 llowing colitis in adult Sox2CreER:YFP mice, YFP initially expressed predominantly by glia becomes ex

145 e with anterogradely labeled CST axons, most YFP-labeled axons beyond established CST locations do no

146 reas among messenger of IFN-beta-BM-mDC most YFP(+) cells were also eGFP(+).

147 FS cell microenvironment, we injected murine YFP(+) embryonic stem cells (ESC) into the amniotic flui

148 , we use two unique mouse strains--an Ndfip1-YFP reporter and an Ndfip1-deficient strain--to show tha

149 h a partner kinase juxtaposes nonfluorescent YFP fragments fused to the C terminus of each protein, r

150 nifested as a marked shift in the normalized YFP/mCherry fluorescence ratio, reliably predicted viral

151 al system; however, high-level ChR2 (but not YFP) expression was associated with substantial cytotoxi

152 , via piggyBac transposition, over 600 novel YFP-trap proteins tagging just under 400 Drosophila loci

153 FRET experiments conducted using Nox1-YFP and NOXA1-CFP illustrate that NoxA1ds disrupts the b

154 We also observed YFP-rhTRIM5alpha within a diversity of structures with c

155 Site-specific protein cleavage of YFP-TRF1 by tobacco etch virus protease resolves telomer

156 CD4 and AP-2 resulted in complementation of YFP and a bright fluorescent signal by confocal microcop

157 Deletion of YFP(+) cells did not alter levels of markers of liver in

158 We further demonstrate that the density of YFP-labeled axon arbors hinders tracing of single axons

159 and spectral overlap between the emission of YFP and the visible-region (QX) absorption bands of the

160 (Pet-1) to drive 5-HT neuronal expression of YFP, we identified 5-HT neurons in live acute slices.

161 Accordingly, a significant fraction of YFP-positive cortical neurons in YFP(J16) mice cortex we

162 o complementary non-fluorescent fragments of YFP and co-expressed in 293T cells.

163 internal reflection fluorescence imaging of YFP-MotB (part of a stator force-generating unit) confir

164 Isolation of YFP(+) CD11b(-) cells from the plug revealed a small sub

165 itive; though cells expressing low levels of YFP were also positive for benzidine, a hemoglobin stain

166 Importantly, the midcell localization of YFP-p1 was disrupted in a strain that does not express F

167 lls promoted plasma membrane localization of YFP-PLCbeta3.

168 elling along the length of the axon, loss of YFP signal, and transected appearance.

169 Loss of YFP(+) NSCs following Hif1a gene inactivation in vivo wa

170 e deletion resulted in a significant loss of YFP(+) NSCs within the SVZ by 45 d post recombination, w

171 In vitro measurements of YFP/CFP fluorescence emission ratios indicated that the

172 esting 1 (LH1) complex shows the position of YFP attachment to the RC-H subunit, on the cytoplasmic s

173 epletion of PARP3 impairs the recruitment of YFP-Ku80 to laser-induced DNA damage sites and induces a

174 lls from the plug revealed a small subset of YFP(+) CD144(+) CD11b(-) E* cells which expressed EC gen

175 n the ischemic hindlimb of a small subset of YFP(+) CD144(+) CD11b(-) fibroblasts (E* cells) that exp

176 to express cyan fluorescent protein (CFP) or YFP fused to either biologically active HCV helicase or

177 infected with lentivirus containing ChR2 or YFP gene and subjected to cytotoxicity analysis.

178 d constructs to be imaged with either GFP or YFP filter cubes.

179 tricular viral injections to express VAPB or YFP throughout the brain and spinal cord of superoxide d

180 At the cellular level, pCkx3::YFP reporter-gene studies revealed that the Ckx3 promote

181 ines expressing the biologically active phyA-YFP photoreceptor in different tissues, and analyzed the

182 is drastically decreased compared with phyB-YFP, and (iii) SUMOylation of phyB inhibits binding of P

183 tage of yellow fluorescent protein-positive (YFP(+)) hepatocytes contained markers of oxidative stres

184 that is prone to aggregation, with prominent YFP-fluorescent aggregates observed in the motor neurons

185 ne encoding the Yellow Fluorescence Protein (YFP) into the dexamethasone inducible vector pOpOff2 and

186 Both 25/26KT Gag-yellow fluorescent protein (YFP) and 29/31KT Gag-YFP bound nonspecifically to the PM

187 en CD44 fused to yellow fluorescent protein (YFP) and CD44 fused to cyan fluorescent protein on K562

188 AtCruA fusion to yellow fluorescent protein (YFP) and expression in developing embryos of A. thaliana

189 lizing IFN-gamma-yellow fluorescent protein (YFP) and IL-10-GFP dual reporter mice, we show that prim

190 eron (IFN-gamma)-yellow fluorescent protein (YFP) and IL-10-green fluorescent protein (GFP) reporter

191 al exon encoding yellow fluorescent protein (YFP) and protein affinity tags.

192 e and female SST-yellow fluorescent protein (YFP) and SST-channelrhodopsin 2 (ChR2)-YFP mice, we quan

193 Both SIS8-yellow fluorescent protein (YFP) and UGT72E1-YFP fusion proteins localize to the nuc

194 tion centre (RC)/yellow fluorescent protein (YFP) complex accelerates photosynthetic growth in the ba

195 T(a) warming in yellow fluorescent protein (YFP) control mice achieved.

196 nd quantified by yellow fluorescent protein (YFP) expression.

197 We expressed yellow fluorescent protein (YFP) from a yeast promoter and selected for a regular al

198 hat a functional yellow fluorescent protein (YFP) fusion of BdCSLF6 is localized to the Golgi apparat

199 conjunction with yellow fluorescent protein (YFP) fusions of Heph and APP family members APP, APLP1,

200 he expression of Yellow Fluorescent Protein (YFP) in these animals is restricted to myeloid lineage a

201 Yellow fluorescent protein (YFP) is often used as an acceptor but YFP is prone to ph

202 ed from IFN-beta yellow fluorescent protein (YFP) reporter mice (messenger of IFN-beta) resulted in Y

203 reported to have yellow fluorescent protein (YFP) selectively expressed in forebrain neurons leading

204 By using yellow fluorescent protein (YFP) translational fusions, CML38 protein was found to b

205 Yellow fluorescent protein (YFP) was present in >96% of hepatocytes before exposure

206 ll when Galphai2 yellow fluorescent protein (YFP) was tethered to the carboxyl terminus of the alpha2

207 c interaction of yellow fluorescent protein (YFP)-tagged beta3 integrin with c(RGDfK) peptide.

208 ssion of TRF1 or yellow fluorescent protein (YFP)-TRF1 fusion protein above endogenous levels prevent

209 rotein (CFP) and yellow fluorescent protein (YFP).

210 rotein (CFP) and yellow fluorescent protein (YFP).

211 axons expressing yellow fluorescent protein (YFP).

212 II (MT-II), and yellow fluorescent protein (YFP).

213 rotein (CFP) and yellow fluorescent protein (YFP)] and FLAG-APP-Myc.

214 functional fluorescent PUB13 fusion protein (YFP-PUB13) localizes to TGN and Golgi compartments and t

215 labeled by GFP (green fluorescent protein), YFP (yellow fluorescent protein), neither, or both.

216 Gene knockout, protein-YFP tags and physiological assays were used to determine

217 ed Medicago truncatula roots, and quantified YFP fluorescence and mRNA levels.

218 ddition, we use SiMPull to directly quantify YFP and mCherry maturation probabilities, showing these

219 al cells (Sox9CreER(T2);Pten(flox/flox);R26R(YFP) or Pten(DeltaDuct/DeltaDuct) mice) and used Pten(De

220 neurons, with Dlx5/6-eGFP and Lhx6-Cre::R26R-YFP being expressed most abundantly in Layer 5, whereas

221 tracing was induced in Lrig1-CreERT2/+;R26R-YFP/+ (Lrig1/YFP) mice that were uninfected or subsequen

222 We generated nestin-CreER(T2)/R26R-YFP/Hif1a(fl/fl) triple transgenic mice, to enable tamox

223 sient absorption spectroscopy of purified RC/YFP complexes show that the YFP-RC intermolecular distan

224 The structure of the RC/YFP-light-harvesting 1 (LH1) complex shows the position

225 Lengths of profiles of regenerating YFP(+) axons were measured 2 wk later from confocal imag

226 luorescent protein (RelA-FP) construct: RelA-YFP, RelA-mEos2 and RelA-Dendra2.

227 R and the Cre-inducible fluorescent reporter YFP.

228 ingly, dexamethasone removal did not reverse YFP inhibition.

229 We treated AAV-TBG-Cre; Rosa(YFP) mice with diethylnitrosamine (DEN), followed by mul

230 xin deleted YFP(+) cells from Foxl1-Cre;Rosa(YFP/iDTR) mice and prevented the resolution of hepatic s

231 Based on studies of Foxl1-Cre;Rosa(YFP/iDTR) mice, Foxl1(+) HPCs and/or their descendants a

232 g HPCs and their descendants (Foxl1-Cre;Rosa(YFP/iDTR)-inducible diphtheria toxin receptor [iDTR] mic

233 causes recombination (AAV-TBG-Cre) into Rosa(YFP) mice.

234 In Kras(G12D)/Pdx1-Cre/Tp53/Rosa(YFP) genetically modified mice, oral administration of S

235 man and mouse (Kras(G12D)/Pdx1-Cre/Tp53/Rosa(YFP)) PDAC cells were incubated with inhibitors of MEK (

236 ing experiments based on Sox18Cre(ERt2)/Rosa-YFP mice.

237 Lineage tracing by using Cdh5cre(ERt2)/Rosa-YFP reporter strategy demonstrated that the CD31-/loVEGF

238 NDCs were isolated from Shh-cre;ROSA:YFP mice at embryonic day 12.5 and postnatal day 0, repr

239 +) and Pdx1Cre;Kras(G12D/+);p53(fl/+);Rosa26(YFP) mice (PDAC), and Pdx1Cre;Kras(G12D/+);p53(fl/+);Spa

240 mice (Pdx1Cre;Kras(G12D/+);p53(fl/+);Rosa26(YFP);Cre;Etv1(fl/fl)) reduced levels of SPARC and hyalur

241 ied out on double-transgenic Wnt1-Cre/ROSA26-YFP mice showing stable YFP expression in all neural cre

242 he coupled protonation reaction, for several YFP variants and detect slow kinetics (dissociation rate

243 pinal cords of paralyzed bigenic mice showed YFP fluorescent inclusion-like structures.

244 ct consequence of vascular regression, since YFP(+) neurosphere formation over serial passage was una

245 Transient expression of a SlCAT9-YFP fusion in tobacco confirmed a tonoplast localisation

246 pinal neurons are labeled with YFP, and some YFP-labeled cells in the spinal gray matter have YFP-lab

247 We show here that in CST-YFP mice, some YFP-labeled axons are not from the CST.

248 Sox2CreER:YFP and PLP1creER:tdT mice were used to determine the fa

249 Following colitis in adult Sox2CreER:YFP mice, YFP initially expressed predominantly by glia

250 Specifically, YFP-labeled axons are present in regions beyond those wi

251 crossover nanostructure that recruits split YFP when properly assembled.

252 lementation (BiFC; also referred to as split-YFP assays) are applicable to the analysis of protein-pr

253 dogenous SRDs-containing proteins and an SRD-YFP fusion localize with AAL to the nuclear membrane.

254 enic Wnt1-Cre/ROSA26-YFP mice showing stable YFP expression in all neural crest-derived cell populati

255 Emx1-Cre x Thy1-STOP-YFP mice have been reported to have yellow fluorescent p

256 TAN1-YFP expressed in tan1 air9 significantly rescued the dou

257 N1 fused to yellow fluorescent protein, TAN1-YFP, and several deletion constructs were transformed in

258 of cortical division site localized TANGLED1-YFP.

259 CLIN1B destruction box was fused to TANGLED1-YFP to generate a line that mostly rescued the division

260 We then cloned a hpRNA targeting YFP under the regulation of the inducible promoters, tra

261 In vivo analysis using a TatA-YFP fusion showed that the TatB F13Y substitution result

262 Under these conditions the TatA-YFP fusion supports full physiological Tat transport act

263 ative stress, DNA damage, or cell death than YFP-negative hepatocytes, indicating that YFP(+) hepatoc

264 roduced changes in cell adhesion rather than YFP expression: clonal populations oscillated between si

265 d CST-YFP mice for 3D imaging and found that YFP fluorescence in CST-YFP mice is faint for clearing-b

266 our days after transplantation we found that YFP(+) sorted cells maintained the expression of pluripo

267 an YFP-negative hepatocytes, indicating that YFP(+) hepatocytes are newly formed cells.

268 y of purified RC/YFP complexes show that the YFP-RC intermolecular distance and spectral overlap betw

269 mbranes as demonstrated by the fact that the YFP-tagged SYP72 localized to the ER in wild-type plants

270 Many of these YFP mutants bind halides with affinities in the millimol

271 ic branches of these neurons in C57/Bl6 Thy1-YFP male mice.

272 YFP(+) BMCs in thy1-YFP mice have immunophenotypic features of MDSCs.

273 ging in comparison with fluorescence in Thy1-YFP-H mice and fluorescence of mini-ruby biotinylated de

274 voxel-based morphometry (VBM) study of Thy1-YFP mice following auditory fear conditioning complement

275 ted into the vitreous humor of B6.Cg-Tg(Thy1-YFP)HJrs/J mice.

276 -smear counts of circulating cells from Tie1-YFP embryos showed that up to 30% of blood-borne cells a

277 133(+)) generate intermediate astrocyte (Tnc(YFP-low) CD15(+)) precursors and GABAergic transient amp

278 ural stem-cell-like primary progenitors (Tnc(YFP-low) CD133(+)) generate intermediate astrocyte (Tnc(

279 the catalytic domain of E3 ligase, CHIP, to YFP-tagged KCNQ1 +/- KCNE1 subunits with a GFP-nanobody

280 nalysis of Sr33 and Sr50 CC domains fused to YFP and either nuclear localization or nuclear export si

281 r phenotype in transgenic mice, was fused to YFP, and fluorescent inclusions were quantified.

282 d plastid localization using AtRBSK fused to YFP.

283 he context of HD in vivo, we bred transgenic YFP(J16) with R6/2 mice, a widely used HD model.

284 yellow fluorescent protein (YFP) and UGT72E1-YFP fusion proteins localize to the nucleus when transie

285 2 to be a suitable tag, with the unamplified YFP signal localizing appropriately to inhibitory synaps

286 changes occur in the anal depressor, we used YFP:actin to monitor, and mutant analysis, laser-ablatio

287 nsfer-based assay (CAMYEL, cAMP sensor using YFP-Epac-Rluc), we assessed the predicted compounds for

288 Cs in a stepwise differentiation process via YFP(-)Ly51(low)CD80(low) intermediates.

289 osis and found that HCA and HCC nodules were YFP(+) lineage-labeled; positive for osteopontin, SRY (s

290 expression constructs (Gag or Gag-YFP, where YFP is yellow fluorescent protein) created from all repr

291 g on the spot with little net movement while YFP macrophages have a more rounded shape and migrate al

292 lymphoid organs and regressing plaques while YFP+ cells were associated with progressing and stable p

293 hese neurons are transgenically labeled with YFP in the 5XY mouse, which enable longitudinal imaging

294 and reticulospinal neurons are labeled with YFP, and some YFP-labeled cells in the spinal gray matte

295 We tagged all 27 Drosophila Rabs with YFP(MYC) at their endogenous chromosomal loci, determine

296 uring oocytes, a function recapitulated with YFP-3'UTR reporters.

297 nohistochemical double labeling studies with YFP and serotonin antisera combined with electron micros

298 notion, HEK293 cells stably transfected with YFP-tagged R753Q TLR2 displayed reduced recruitment of M

299 between a constitutively active phyB(Y276H)-YFP allele (YHB-YFP) and PCH1, we show that the loss of

300 itutively active phyB(Y276H)-YFP allele (YHB-YFP) and PCH1, we show that the loss of PCH1 prevents YH

301 mpromises a number of events elicited in YHB-YFP plants, including their constitutive photomorphogeni